rs1799971, OPRM1

N. diseases: 95
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.040 GeneticVariation BEFREE There was no statistically significant difference in genotypic and allelic frequencies of OPRM1 A118G SNP between HCs and SZ/BD patients. 29497192 2019
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.040 GeneticVariation BEFREE Compared with the A allele of rs</span>1799971 and C allele of rs2075572, the G allele of rs1799971 and rs2075572 was associated with an almost 0.46-fold risk (OR=0.46, 95% CI: 0.357-0.59, P<0.01) and 0.7-fold risk (OR=0.707, 95% CI: 0.534-0.937, P=0.015) of the occurrence of SZ,. 23560613 2013
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.040 GeneticVariation BEFREE The A118G polymorphism may also be associated with substance dependence and susceptibility to other disorders, including epilepsy and schizophrenia. 21919606 2011
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.040 GeneticVariation BEFREE The study was focused on the relationship between the functional A118G polymorphism of the OPRM1 gene (rs1799971) and schizophrenia in groups of 130 male patients and 452 male controls. 20112002 2010